Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F257/00—Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00
  • C08F257/02—Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00 on to polymers of styrene or alkyl-substituted styrenes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S525/902—Core-shell

Definitions

• This invention relates to elastomers and more particularly to elastomeric compositions comprising a rigid copolymer and a rubbery copolymer and to a method for the preparation thereof. Still more particularly, this invention relates to elastomeric compositions having a core-shell structure prepared by a sequential polymerization process, said compositions comprising (a) a rigid copolymer core formed of at least one rigid monovinylidene monomer and a first copolymerizable functional monomer; said rigid copolymer having a glass transition temperature of greater than 20°C, (b) a rubbery copolymer outer layer or shell formed of at least one rubbery acrylic monomer and a second copolymerizable functional monomer, said rubbery copolymer having a glass transition temperature of less than about 0°C, and (c) a transition layer, intermediate between the core and outer shell, formed of a mixture of the core components and the outer shell components.
• Patent 3,265;765 possess the necessary elastomeric properties without curing and are permanently thermoplastic and soluble.
• These and related thermoplastic block copolymers have found wide'commercial acceptance in part because of their ready reprocessability.
• the method of their preparation involves an anionic solution polymerization process which inherently is limited to use with a narrow spectrum of anionically polymerizable hydrocarbon monomers. Because such polymers are readily dissolved by low molecular weight hydrocarbons they do not exhibit good oil and solvent resistance. Additionally, these hydrocarbon elastomers are subject to other environmental attack and particularly to degradation by UV radiation because of the presence of ethylenic unsaturation and are unsuited for outdoor use without substantial stabilizing or further treatment.
• Acrylic elastomers have long been known for their heat stability and resistance to oil. These materials are prepared from acrylic esters such as ethyl acrylate and butyl acrylate and must be thermally or chemically crosslinked to impart the necessary strength properties. Emulsion polymerization processes have been widely employed for the production of acrylic elastomers and methods for chemical crosslinking of these materials with difunctional monomers are well known. As with conventional elastomers, these materials are insoluble and difficult to reprocess after being cured. More recently, a thermoplastic acrylic elastomer has become known as was disclosed in Shah, et al, U.S. Patent 4,306,039.
• elastomers are blends of a rubbery acrylic copolymer containing an acidic functional monomer with a rigid polymer of an N-vinyl lactam. Although the resulting elastomers are said to be oil resistant, reprocessable thermoplastics, the compositions are limited to blends of acrylic rubbers with N-vinyl lactam polymers. Altering the balance of properties to reduce water sensitivity or change other physical characteristics by the incorporation of additional monomers is not readily acheived.
• Elastomers having a core-shell structure have also been disclosed in the prior art.
• the term core-shell structure has become well-understood in the art as defining a layered particulate composition having a polymeric center or core surrounded and encapsulated by a shell or overcoat formed of a second polymeric material.
• Methods for the preparation of such core-shell particulate compositions are now well known in the art and include a variety of layered particulate materials having a core and one or more shell layers.
• inUS-A-3,661,994 graft polymers formed by a sequential polymerization process are disclosed wherein a rigid, polymeric seed or core is surrounded by a graft polymerized rubber layer and, optionally, encapsulated with a graft polymerized rigid outer layer.
• core-shell description of these particulate compositions is intended to describe the product of the polymerization process; fusion of the shell component occurs during thermal processing such that the core-shell nature of the product is no longer discernable.
• the resulting particulate materials are useful as reinforcers and impact modifiers for plastics.
• an acrylic elastomer is prepared by sequentially graft polymerizing monomers to form an acrylic elastomer shell in the presence of and encapsulating a rigid, particulate cross-linked polymeric core.
• These elastomers may further include complementary reactive monomers in the rigid and rubbery layers that interact by a condensation reaction in a subsequent curing step to bond the layers and effect a further crosslinking of the rubbery layer. The resulting acrylic elastomers are thus cured during processing and are not truly reprocessable.
• thermoplastic composition having elastomeric properties which could be prepared by a low cost emulsion process from readily available monomers and which could be varied over a wide composition range to alter the balance of physical properties to meet varied end use requirements would thus be a substantial advance in the elastomer art.
• This invention is a thermoplastic elastomeric composition
• a rigid copolymer core formed of at least one rigid monovinylidene monomer and a first copolymerizable functional monomer, said rigid copolymer having a glass transition temperature greater than 20°C
• a rubbery copolymer outer shell prepared in the presence of and at least partially encapsulating the preformed core copolymer, said shell formed of at least one rubbery acrylic monomer and a second copolymerizable functional monomer, said rubbery copolymer having a glass transition temperature of less than about 0°C
• a transition layer intermediate between the core and outer shell formed of a mixture of the core and shell components.
• the copolymerizable functional monomers are monoethylenically-unsaturated monomers containing at least one reactive, non-vinylic functional radical, and the first and second copolymerizable monomers are selected to be interreactive through their respective functional radicals.
• the compositions of this invention are thermoplastic elastomers without being vulcanized or cured, thus remaining thermally reprocessable.
• the rigid copolymers useful in forming the particulate core copolymer in the compositions of this invention are copolymers of at least one rigid monovinylidene monomer and a first copolymerizable functional monomer.
• the term rigid is a misnomer when applied to monomers, and what is meant by the phrase rigid monovinylidene monomers are monomers that when polymerized will provide a rigid polymer having a glass transition temperature (Tg) greater than 20°C and include vinyl aromatic monomers, acrylic monomers, and copolymerizable mixtures thereof.
• vinyl aromatic monomers examples include styrene, alpha methylstyrene, alkyl-substituted styrene monomers such as vinyl toluene and halogen- substituted styrene monomers such as chlorostyrene, bromostyrene, di-and tri-bromo styrene and the like, and illustrative of acrylic monomers are alkyl methacrylates including methyl methacrylate, butyl methacrylate, octyl methacrylate and the like, and the corresponding nitriles such as acrylonitrile, methacrylonitrile, haloacrylonitrile and the like.
• the core copolymer may further include a copolymerizable, non-rigid monovinylidene monomer such as for example an alkyl acrylate, a vinyl ether, a vinyl ester or the like in minor amounts insufficient to depress the Tg of the final rigid copolymer below 20°C.
• a copolymerizable, non-rigid monovinylidene monomer such as for example an alkyl acrylate, a vinyl ether, a vinyl ester or the like in minor amounts insufficient to depress the Tg of the final rigid copolymer below 20°C.
• the core copolymer further includes at least one copolymerizable functional monomer, defined as a monoethylenically unsaturated monomer containing at least one reactive, non-vinylic functional radical.
• the functional radi-cal may be selected from the group consisting of epoxy radicals, carbonyl radicals such as carboxylic acid, carboxylic anhydride, carbonamide, N-substituted carbonamide, aldehyde, alkyl and aryl keto, and the like, hydroxyl radicals, thiol radicals, amino radicals, isocyanate radicals, alkoxyalkyi radicals, and the like.
• Such functional monomers include glycidyl methacrylate, acrylic and methacrylic acids, maleic anhydride, maleimide, acrylamide, N-alkoxyalkyl acrylamides such as N-isobutoxymethyl acrylamide, N-hydroxymethyl acrylamide and the like, methyl vinyl ketone, acrolein, vinyl isocyanate, hydroxyalkyl acrylates such as 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate and the like. Also included are mixtures of two or more such functional monomers.
• the core copolymers may be varied over a wide composition range, however, for most purposes the copolymer will comprise from about 99.9 to about 95 wt% of at least one rigid monovinylic monomer and from about 0.1 to about 5 wt% of first copolymerizable functional monomer.
• the preferred core copolymers are copolymers of styrene, acrylonitrile and acrylic acid.
• the rubbery copolymers useful as the shell copolymer in the compositions of this invention are copolymers of at least one rubbery acrylic monomer and a second copolymerizable functional monomer.
• rubbery acrylic monomers is intended to mean monomers that when polymerized will provide a rubbery polymer having a Tg below about 0°C.
• Illustrative of rubbery acrylic monomers are the alkyl acrylates including ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, and the like.
• the rubbery copolymer may further include any of the rigid monovinylidene monomers set forth above such as for example styrene, acrylonitrile, methyl methacrylate and the like in amounts insufficient to raise the Tg of the final rubbery copolymer above about 0°C, which amount will lie in the range of from 0 to 100 parts by weight of rigid monovinylidene monomer per 100 parts by weight of rubbery monomer.
• the shell copolymer further includes a second copolymerizable functional monomer, defined as a monoethylenically unsaturated monomer containing at least one reactive functional radical.
• the second functional monomer may be any of those defined hereinabove as useful for the preparation of the core copolymer including mixtures containing two or more such functional monomers, with the proviso that the reactive functional radical of said second functional monomer must be capable of reacting with the reactive functional radical of the first functional monomer contained in the core copolymer.
• the reactive functional monomer contained within the core copolymer and the reactive functional monomer contained within the shell copolymer are complementary or interreactive.
• the shell copolymer may optionally further include a minor amount of a copolymerizable di- or trivinyl monomer such as a glycol diacrylate, divinylbenzene, trialkylcyan- urate or the like to provide further grafting sites, as is widely practiced in the art.
• a copolymerizable di- or trivinyl monomer such as a glycol diacrylate, divinylbenzene, trialkylcyan- urate or the like to provide further grafting sites, as is widely practiced in the art.
• the shell copolymer may be varied over a wide composition range, however, for most purposes the copolymer will comprise from about 99.9 to about 95 wt% of at least one rubbery monomer and from about 0.1 to about 5 wt% of second copolymerizable functional monomer.
• the preferred shell copolymers are copolymers of an alkyl acrylate and 2-hydroxyethyl methacrylate.
• the transition layer will be a copolymer formed from a mixture of the rubbery shell copolymer components and the rigid core copolymer components.
• the thermoplastic elastomeric compositions of this invention may be varied widely in the proportion of rigid core copolymer component and rubbery shell copolymer component as well as in the proportion of each that will be incorporated into the transition layer.
• the ratio of rigid copolymer component to rubbery shell copolymer component will lie in the range of from about 1:10 to about 1:1, i.e., the composition will be comprised of from about 10 to about 100 parts by weight of the rigid copolymer component per 100 parts by weight of the rubbery copolymer component.
• compositions having a ratio above or below this range may well have utility where good elastomeric properties are not important.
• the proportion of rigid core, transition layer and rubbery shell in the final core-shell particle may also be varied over a wide range.
• the transition layer will comprise from about 20 to about 80 wt% of the total weight of the core-shell particle structure.
• the resulting elastomer has low tensile properties and poor low temperature characteristics, while at very high proportions of transition layer, the elastomer loses rubbery character.
• the proportion of transition layer will vary depending upon the ratio of rigid core copolymer to rubber shell copolymer employed, the preferred compositions will have from about 30 to about 70 wt% transition layer in the final core-shell particle structure.
• compositions of this invention are prepared by an emulsion process, and preferably by a sequential emulsion polymerization process in which as a first polymerization step the core copolymer is prepared in particulate form as a latex.
• the transition layer is then formed by adding the monomers of the core and shell copolymers to the latex simultaneously, and polymerizing under conditions designed to minimize the formation of new particles, thus surrounding and encapsulating or partially encapsulating the particles of rigid core copolymer with the mixed polymers forming the transition layer.
• the monomers of the shell copolymer component are added and polymerized to form the encapsulating outer shell.
• the staged process is analogous to the seeded sequential emulsion processes long known and used in the art to prepare multi-layered or core-shell polymer particles comprising highly crosslinked rubber phases either surrounding or encapsulated by other cross-linked polymeric layers.
• Typical of such processes are those disclosed by Hwa, et al in U.S. patent 3,661,994 and by Minton, in U.S. patent 3,502,745.
• These sequential processes may be adapted to the preparation of the uncrosslinked and thermoplastic elastomeric compositions of this invention to provide the desired core-shell layered particles having a rigid core, a mixed transition layer and a rubbery outer shell.
• thermoplastic elastomer compositions of this invention will preferably be directly prepared from the monomers by a sequential emulsion polymerization process
• the- requisite reactive functionality may be introduced by a post-reaction.
• a controlled partial hydrolysis of an acrylate ester polymer such as a methyl methacrylate-styrene copolymer may be employed to provide a rigid core copolymer having carboxylic acid radicals.
• equivalent polymers could be obtained by hydrolysis of styrene-vinyl acetate or styrene-maleic anhydride copolymers to provide rigid core copolymers having pendant hydroxyl or carboxylic acid radicals.
• Oxidation and epoxidation of ethylenically-unsaturated polymers may also be employed to introduce reactive hydroxyl, carboxylic or epoxy functionality.
• Rigid core copolymers may also be prepared by other methods and converted to the emulsion form for subsequent use in grafting by processes well known in the art.
• thermoplastic compositions of this invention thus comprise a particulate core formed of rigid core copolymer components, an outer shell formed of rubbery shell copolymer components and a transition layer intermediate between the core and outer shell, formed of a mixture of the core copolymer components and the shell copolymer components.
• the rigid core copolymer, the transition layer copolymers and the rubbery shell copolymer are capable of forming further bonds in a reaction between their respective functional radicals.
• the relative proportion of functional monomer present in each phase and the ease with which they interreact will affect the degree of linking and in turn may affect the reprocessability of the compositions.
• the optimum or most favorable functional monomer content will depend in part upon the particular end use requirement for ready moldability and reprocessability and will necessarily be determined for each particular combination of interreactive or complementary functional monomers by experiment. Thus, although functional monomer levels as great as 20 wt% may in some combinations produce thermally processable compositions, where higher degrees of processability and reprocessability are required, functional monomer levels of less than 5 wt% will be preferred.
• the linking reaction will preferably take place after preparation of the core-shell structure, such as for example under the conditions encountered during a conventional melt-compounding or thermal processing step, i.e. during extrusion, milling or molding of the thermoplastic elastomeric composition.
• compositions of this invention will be useful in the production of molded and extruded articles without further compounding, as a practical matter these compositions will normally be further compounded with stabilizers, fillers, pigments, dyes, extenders, lubricants and processing aids for use in particular applications.
• a metal oxide or carbonate such as with from 0.1 to 1.0 wt% of zinc oxide, calcium oxide, sodium carbonate or the like, improves the extrusion and molding characteristics of these compositions.
• a metal oxide or carbonate such as with from 0.1 to 1.0 wt% of zinc oxide, calcium oxide, sodium carbonate or the like.
• the compositions of this invention will also be useful as impact modifiers for a wide variety of thermoplastic resins, including polystyrene, styrene-acrylonitrile resins, vinyl resins, polyethers, polyesters, and the like.
• thermoplastic elastomer compositions of this invention will be better understood by consideration of the following examples which are provided by way of illustration and not in limitation thereof.
• reaction mixtures were prepared, degassed, and stored under nitrogen prior to polymerization:
• a 5 1. polymerization reactor was charged with a mixture of 1350 g of water, 3.0 g. of sodium carbonate and 1.4 g. of DS-4 (sodium dodecyl benzene sulfonate, 23% aqueous). The mixture was stirred under a nitrogen atmosphere and heated to 80°C, then 97.5 of the rigid monomer emulsion was added, followed by 100 ml of the initiator solution. After stirring at 250 rmp and 80°C for 30 min., an additional 146.3 g. of the rigid monomer emulsion was added over a 10 min. period, and the stirred mixture was heated at 80°C an additional 10 min., to complete the formulation of the particulate core copolymer latex.
• DS-4 sodium dodecyl benzene sulfonate
• a "chaser" mixture of 1 ml of 75% t-butyl peroxy pivalate, 5.2 ml of 5% sodium formaldehyde sulfoxylate and 5 ml of water may be added at this point to reduce the unreacted monomer levels.
• the cooled latex was filtered, then coagulated by slowly stirring into 4 volumes of dilute aqeuous aluminum sulfate.
• the solid polymer was then collected by centrifugation, washed with water and dried overnight at 40-50°C in a vacuum oven.
• the composition is a core-shell composition having 18.8% core of a rigid core copolymer of 97.3 wt% styrene and acrylonitrile as monovinylidene monomers and 2.7 wt% acrylic acid as the first functional monomer, and 30.2% of a rubbery shell copolymer of 96.8 wt% butyl acrylate as the rubbery monomer and 2 wt% of 2-hydroxyethyl methacrylate as the second functional monomer.
• the intermediate or transition layer comprises 50.3 wt% of the structure, and is a mixture of the styrene, acrylonitrile and acrylic acid rigid core monomer components and the butylacrylate and 2-hydroxyethyl methacrylate rubbery shell monomer components.
• the ratio of rigid copolymer components to rubbery copolymer components is 1:1.67, corresponding to 60 pbw (parts by weight) rigid components per 100 pbw rubber components in the composition.
• compositions having varying levels of the rubbery copolymer component were prepared substantially by the process set forth in Example 1 by varying the rigid and rubbery monomer levels as well as the functional monomer content and proportion of intermediate layer.
• Control Examples A-F were prepared substantially by the process set forth in Example 1, but omitting a particular layer or layers or the functional monomers.
• compositions were compounded with from 0.1 to 0.5 pbw zinc oxide per hundred parts of the elastomer, milled at room temperature, sheeted out and cut into strips. The milled strips were then fed to a Brabender 3/4 in. (19.05 mm) extruder and extruded using barrel and die temperatures in the range 160-171°C. The chopped extrudate was injection molded in a Battenfeld 1 1/2 oz. screw injection molding machine using barrel and nozzle temperatures in the range 149-177°C and a mold temperature of 27-32°C to provide test specimens.
• compositions of this invention exhibit desirable and useful properties. That the presence of a core layer, a shell layer and a transition layer is essential to attaining good elastomeric properties will be seen by a comparison of Examples 1 and 2 with Control Examples A-E having equivalent overall compositions. Omitting the shell layer (Control A), or the core and shell layers (Control B) results in an elevation in brittle point temperature, substantially limiting the low temperature properties of the elastomer. Additionally, omitting the transition layer (Control C) results in soft, low strength gum, while omitting the core layer (Controls D & E) provides a substantially less elastomeric product.
• Example 1 Within a given composition range, lowering the level of transition layer decreases the tensile strength of the resulting product. Compare Example 1 with 2 and Example 3 with 4. As will be seen by a comparison of Examples 2, 3 and 8 and of Examples, 5-7, and Control F, at a given level of core, shell and transition layer, decreases in reactive monomer level tend to produce decreases in tensile strength, with minor increases in elongation. Without functional monomer, however, the product is a low strength gum (Control F).
• Example 9-13 prepared substantially by the process of Example 1, the level of rigid monomers was varied. The formulations and physical properties are summarized in Table II.
• the levels of rigid monomer component, reactive monomer content and relative proportion of core, shell and transition layer may thus be selected over a wide range to provide the elasticity, hardness, tensile properties and solvent resistance properties desired for particular end-uses.
• Example 14-18 prepared substantially by the process of Example 1, the composition-of the rigid and rubbery monomers was varied. The compositions and their physical properties are summarized in Table III.
• composition having a core-shell structure comprising (a) a rigid copolymer core formed of at least one rigid monovinylidene monomer and a first copolymerizable functional monomer, said rigid copolymer having a glass transition temperature greater than 20°C, (b) a rubbery copolymer outer shell formed of at least one rubbery acrylic monomer and a second copolymerizable functional monomer, said rubbery copolymer having a glass transition temperature of less than about 0°C, and (c) a transition layer formed of a mixture of the core and shell monomer components.
• the shell copolymer (b) surrounds and partially encapsulates the core copolymer (a), and the transition layer is intermediate between the core and shell components.
• compositions of this invention are useful as moldable and extrudable elastomers, and may be further compounded with pigments, processing aids, stabilizers, antioxidants, lubricants, fillers, plasticizers and the like as is commonly practiced in the rubber compounding art without departing from the scope of the invention.

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• 1983
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